- Chemical Name:R-ALPHA-AMINO-4-METHOXYBENZENE ACETAMIDE
- CAS No.:67412-96-8
- Molecular Formula:C9H12N2O2
- Molecular Weight:180.206
- Hs Code.:2906190090
Synonyms:D-p-methoxyphenylglycine amide;PS-J-111;
Synonyms:D-p-methoxyphenylglycine amide;PS-J-111;
98%Min *data from raw suppliers
(R)-2-AMINO-2-(4-METHOXYPHENYL)ACETAMIDE 95.00% *data from reagent suppliers
There total 5 articles about R-ALPHA-AMINO-4-METHOXYBENZENE ACETAMIDE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
Reference yield: 45.0%
Reference yield:
Reference yield:
2-amino-2-(4-methoxyphenyl)acetamide
2-(R)-(4-methoxyphenyl)-2-[2-(4-methoxyphenyl)acetylamino]-acetamide
The research focuses on the asymmetric synthesis of (S)-CPPG, a selective antagonist for group III metabotropic glutamate receptors (mGluRs), which are important in studying neurotransmission mechanisms. The synthesis begins with (R)-4-benzoxyphenylglycine and involves several steps including protection of the amino group, formation of trans-oxazolidinone, introduction of a dicarbon functional group, and cyclopropanation. Key reactants include methyl chloroformate, benzaldehyde dimethyl acetal, boron trifluoride etherate, and various catalysts for cyclopropanation. The process involves recrystallization, HPLC, and 1H NMR for analysis, and culminates in the production of (S)-CPPG with a final yield of 99% after purification. The study also mentions the biological evaluation of the synthesized compound, indicating ongoing research into its physiological effects.